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The New Phytologist|January 23, 2018
High intraspecific genome diversity in the model arbuscular mycorrhizal symbiont Rhizophagus irregularisEric C H Chen, Emmanuelle Morin, Denis Beaudet, et al.Pediatrics|December 3, 2008
Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysisXin-Yan Lu, Mai T Phung, Chad A Shaw, et al.Genome Research|May 21, 2013
Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing allelesPhilip M Boone, Ian M Campbell, Brett C Baggett, et al.Nature Biotechnology|October 15, 2010
The NIH Roadmap Epigenomics Mapping ConsortiumBradley E Bernstein, John A Stamatoyannopoulos, Joseph F Costello, et al.Prenatal Diagnosis|October 26, 2018
Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testingLiesbeth Vossaert, Qun Wang, Roseen Salman, et al.The Journal of Clinical Investigation|February 18, 2014
Conjugation of a brain-penetrant peptide with neurotensin provides antinociceptive propertiesMichel Demeule, Nicolas Beaudet, Anthony Régina, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|August 24, 2010
A neurodevelopmental survey of Angelman syndrome with genotype-phenotype correlationsJennifer K Gentile, Wen-Hann Tan, Lucia T Horowitz, et al.Human Molecular Genetics|January 15, 1999
The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.American Journal of Medical Genetics. Part A|July 30, 2008
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 casesLina Shao, Chad A Shaw, Xin-Yan Lu, et al.Plos One|March 29, 2007
Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal casesXinyan Lu, Chad A Shaw, Ankita Patel, et al.Pageof 105